Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038700849

FEI Number

3038700849

Entity Name

BEZALEL INNOVATIONS

City/State/Country

Palo Cedro, CA, US

Establishment Address

21810 Oak Meadow Rd, Palo Cedro, CA 96073, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Bezalel Innovations (Owner Number: 10093522)

Owner / Operator Contact Address

21810 Oak Meadow Rd, Palo Cedro, CA 96073, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ACTS 1912

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCY	Tourniquet, Pneumatic	General, Plastic Surgery	Class 1	878.5910	2025-05-28

Official Correspondent

Pieter Lagaay

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bezalel Innovations

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038700849. Last updated year: 2026. Please use registration number 3038700849 when referencing this establishment in official correspondence.